Výsledky vyhledávání - "Chittapragada Maruthi"

Akademický článek

Aminoglycosides: Molecular Insights on the Recognition of RNA and Aminoglycoside Mimics.

Autor: Chittapragada, Maruthi¹, Roberts, Sarah¹, Young Wan Ham¹ yham@chem.byu.edu

Publikováno v: Perspectives in Medicinal Chemistry. 2009, Issue 3, p21-37. 17p. 11 Diagrams, 1 Chart.

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Synthesis of (4R,6S,7R)-7-hydroxy-4,6-dimethyl-3-nonanone and (3R,5S,6R)-6-hydroxy-3,5-dimethyl-2-octanone

Autor: Chitti Srinivas, Jhillu S. Yadav, Gowravaram Sabitha, Chittapragada Maruthi

Publikováno v: Tetrahedron: Asymmetry. 22:2071-2079

The synthesis of (4 R ,6 S ,7 R )-7-hydroxy-4,6-dimethyl-3-nonanone and (3 R ,5 S ,6 R )-6-hydroxy-3,5-dimethyl-2-octanone is described as their acetates using a desymmetrization strategy as well as an Evans syn aldol strategy.

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::92e62d3fe93588fbc11db25de06c4a0b
https://doi.org/10.1016/j.tetasy.2011.11.013

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Enantioselective Synthesis of Herbarumin III by Using a Chelation-Controlled Reduction

Autor: Chitti Srinivas, Jhillu S. Yadav, Chittapragada Maruthi, Gowravaram Sabitha

Publikováno v: Helvetica Chimica Acta. 93:1634-1640

The total synthesis of herbarumin III (1) was achieved via an alkynide ion addition onto a chiral aldehyde and LiAlH4/LiI reduction as key steps (Scheme 2).

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::fad823213563e8702f3824e69feb3fec
https://doi.org/10.1002/hlca.200900427

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Enantioselective Total Synthesis of the Antifungal Agent (6S)-5,6-Dihydro-6-[(2R)-2-hydroxy-6-phenylhexyl]-2H-pyran-2-one

Autor: M. Rajkumar, Chitti Srinivas, Chittapragada Maruthi, Gowravaram Sabitha, Jhillu S. Yadav, Kadari Sudhakar

Publikováno v: Synthesis. 2007:3886-3890

An enantioselective route for the synthesis of (6 S)-5,6-dihydro-6-[(2 R)-2-hydroxy-6-phenylhexyl]-2 H-pyran-2-one is reported. The synthesis is based on epoxide ring opening with a Grignard reagent and stereoselective reduction employing catecholbor

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::a9f225cabffa1f39abec7a61d371356d
https://doi.org/10.1055/s-2007-990928

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Intramolecular Hetero-Diels–Alder Reactions Catalyzed by BiCl3: Stereoselective Synthesis of Benzo-Annelated Decahydrofuro[3,2-h][1,6]naphthyridine Derivatives

Autor: Chitti Srinivas, Jhillu S. Yadav, Ajit C. Kunwar, Erigala Venkata Reddy, Gowravaram Sabitha, Samit Kumar Dutta, Chittapragada Maruthi

Publikováno v: Helvetica Chimica Acta. 89:2728-2731

A novel, efficient synthesis of a series of functionalized, benzo-annelated decahydrofuro[3,2-h][1,6]naphthyridine derivatives 3 has been achieved. The protocol is based on the intramolecular hetero-Diels–Alder (IMHDA) reaction of in situ formed im

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::6975905b83822f74591740de45a24c54
https://doi.org/10.1002/hlca.200690243

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